NM_001387025.1(GRAMD1B):c.2286C>T (p.Ser762=) AND GRAMD1B-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 19, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003911891.2
Allele description [Variation Report for NM_001387025.1(GRAMD1B):c.2286C>T (p.Ser762=)]
NM_001387025.1(GRAMD1B):c.2286C>T (p.Ser762=)
Condition(s)
- Name:
- GRAMD1B-related disorder
- Synonyms:
- GRAMD1B-related condition
- Identifiers:
-
Homo sapiens family with sequence similarity 86 member E, pseudogene (FAM86EP), ...
Homo sapiens family with sequence similarity 86 member E, pseudogene (FAM86EP), transcript variant 3, non-coding RNAgi|751130528|ref|NR_130742.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024